Stryker Sustainability Solutions, Inc. is one of 5299 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Stryker Sustainability Solutions, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Stryker Sustainability Solutions, Inc. has 2 FDA 510(k) cleared medical devices. Based in Phoenix, US.
Historical record: 2 cleared submissions from 2012 to 2013. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Stryker Sustainability Solutions, Inc. Filter by specialty or product code using the sidebar.
Stryker Sustainability Solutions, Inc. — FDA 510(k) Products and Clearance History
2 devices
Cleared
Jan 24, 2013
REPROCESSED STEERABLE INTRODUCER
Cardiovascular
90d
Cleared
Dec 20, 2012
REPROCESSED ULTRASOUND INTRACARDIAC ECHO CATHETER
Cardiovascular
171d